FDA.reportPublic FDA data

APAP

Product NDC
17714-013
Requested package NDC
17714-013-10
11-digit product format
177140013
Labeler code
17714
Product ID
17714-013_60f41580-e099-faad-e053-2a91aa0a9076
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET
Route
ORAL
Labeler
Advance Pharmaceutical Inc.
Application
part343
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
1989-02-05
Substance
ACETAMINOPHEN
Active strength
500 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
APAPACETAMINOPHENAdvance Pharmaceutical Inc.aba26f0a-94e4-4919-a3b0-033e3a9598ef2017-12-22WarningsExact identifier
ndc (package): 17714-013-10
ndc (product): 17714-013
ndc11 (package): 17714001310

Additional Listing Data#

Finished product
Yes
Brand name base
APAP
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACETAMINOPHEN500 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
362O9ITL9DInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
198440Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
aba26f0a-94e4-4919-a3b0-033e3a9598efAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17714-013-01APAP100 in 1 BOTTLETABLET1002
17714-013-10APAP1000 in 1 BOTTLETABLET10002

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ACETAMINOPHENACTIVE INGREDIENT362O9ITL9DAPAP (ACETAMINOPHEN) TABLET [ADVANCE PHARMACEUTICAL INC.]1
ACETAMINOPHENACTIVE MOIETY362O9ITL9DAPAP (ACETAMINOPHEN) TABLET [ADVANCE PHARMACEUTICAL INC.]1
POVIDONEINACTIVE INGREDIENTFZ989GH94EAPAP (ACETAMINOPHEN) TABLET [ADVANCE PHARMACEUTICAL INC.]1
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2APAP (ACETAMINOPHEN) TABLET [ADVANCE PHARMACEUTICAL INC.]1
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJAPAP (ACETAMINOPHEN) TABLET [ADVANCE PHARMACEUTICAL INC.]1
STEARIC ACIDINACTIVE INGREDIENT4ELV7Z65APAPAP (ACETAMINOPHEN) TABLET [ADVANCE PHARMACEUTICAL INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17714-013APAP (ACETAMINOPHEN) TABLET [ADVANCE PHARMACEUTICAL INC.]2Current NDC, Legacy NDC, 2 package rows20171223_aba26f0a-94e4-4919-a3b0-033e3a9598ef.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198440acetaminophen 500 MG Oral TabletPSNaba26f0a-94e4-4919-a3b0-033e3a9598ef2
198440acetaminophen 500 MG Oral TabletSCDaba26f0a-94e4-4919-a3b0-033e3a9598ef2
198440APAP 500 MG Oral TabletSYaba26f0a-94e4-4919-a3b0-033e3a9598ef2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
17714-013-10177140013101000 TABLET in 1 BOTTLE (17714-013-10) 1000 tablet1989-02-050000-00-00NoNoCurrent